Literature DB >> 11678712

Synthesis of an orthogonally protected precursor to the glycan repeating unit of the bacterial cell wall.

S L Saha1, M S Van Nieuwenhze, W J Hornback, J A Aikins, L C Blaszczak.   

Abstract

[reaction: see text]. A synthesis of stereochemically pure and orthogonally protected N-acetyl-(2-deoxy-2-aminoglucopyranosyl)-beta-[1,4]-N-acetylmuramyl (NAG-NAM) monopeptide (2), the glycopeptide core of lipid II and of the bacterial cell wall repeating unit, is reported.

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Year:  2001        PMID： 11678712     DOI： 10.1021/ol016692t

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

1.  Synthesis of Substrates and Biochemical Probes for Study of the Peptidoglycan Biosynthetic Pathway.

Authors:  Radha S Narayan; Michael S Vannieuwenhze
Journal:  European J Org Chem       Date:  2007-01-19

2.  Antimicrobial lipopeptide tridecaptin A1 selectively binds to Gram-negative lipid II.

Authors:  Stephen A Cochrane; Brandon Findlay; Alireza Bakhtiary; Jeella Z Acedo; Eva M Rodriguez-Lopez; Pascal Mercier; John C Vederas
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-29       Impact factor: 11.205

3.  Chemoenzymatic syntheses of water-soluble lipid I fluorescent probes.

Authors:  Katsuhiko Mitachi; Shajila Siricilla; Lada Klaic; William M Clemons; Michio Kurosu
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

4.  One-pot protection-glycosylation reactions for synthesis of lipid II analogues.

Authors:  Katsuhiko Mitachi; Priya Mohan; Shajila Siricilla; Michio Kurosu
Journal:  Chemistry       Date:  2014-03-12       Impact factor: 5.236
  4 in total

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